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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 486694Generated: October 26, 2026

Formaldehyde → HCID 22414444, compound

https://huagongshe.com/reaction/486694

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-amino-N-formyl-N-methyl-alpha-(3-methyl-2-thienyl)benzeneethanamineHCID 10423492—
SolventAcetonitrileHCID 6342—
ProductHCID 22414444HCID 22414444—

Reaction Steps

A solution of 5.0 g of 2-amino-N-formyl-N-methyl-α-(3-methyl-2-thienyl)benzeneethanamine in 48 ml of acetonitrile was treated with 6.5 ml of a 37% formaldehyde solution and 1.9 g of sodium cyanoborohydride. The mixture was stirred for 1.5 hr and then concentrated. The residue was dissolved in 75 ml of ether and washed with 1N potassium hydroxide solution and with saturated brine. The ether solution was dried over anhydrous potassium carbonate and concentrated. The residue was purified by Preparative HPLC (Waters Associates Prep LC/System 500, silica gel, eluted with ethyl acetate, 200 ml/min, Glo-Mac Model 80-800 UV detector). The appropriate fractions were collected and concentrated to give 3.8 g of product, as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05292760
Source datasetuspto-grants-1994_03
ORD IDord-294537446c1e4d988af467a7ba545d11
Source noteuspto-grants-1994_03